HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264836Generated: November 1, 2026
Hydrochloric Acid → 4-cyano-2,2-bisfluoromethyl-6-nitro-2H-1-benzopyran
https://huagongshe.com/reaction/264836
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 2,2-bisfluoromethyl-3,4-dihydro-6-nitro-2H-1-benzopyran-4-one | HCID 15545853 | — |
| Catalyst | zinc(II)iodide | HCID 9883512 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 4-cyano-2,2-bisfluoromethyl-6-nitro-2H-1-benzopyran | HCID 21194980 | — |
Reaction Steps
To a mixture of 4.05 g of 2,2-bis(fluoromethyl)-3,4-dihydro-6-nitro-2H-1-benzopyran-4-one and 10 ml of dried benzene was added 2.52 ml of trimethylsilyl cyanide with stirring under ice-cooling. 0.82 g of zinc iodide was added therein and the mixture was stirred at room temperature for 12 hours. Further, 8 ml of pyridine and 4.41 ml of phosphorus oxychloride were added therein and the resultant mixture was refluxed with heating for 6 hours. Ice water was added to the residue and it was acidified to be hydrochloric acid and it was extracted with methylene chloride. An organic layer was washed with water and dried, and the solvent was distilled. The obtained residue was purified according to silica gel column chromatography (developing solution, CH2Cl2 :hexane=7:3) to obtain 0.99 g of 4-cyano-2,2-bis(fluoromethyl)-6-nitro-2H-1-benzopyran with a melting point of 136°-137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646308 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-07154dedc489443eb097a9500e574f78 |
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| Source note | uspto-grants-1997_07 |
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